(R)-1-(3-Methoxyphenyl)ethanamine

98%

Reagent Code: #230473
fingerprint
CAS Number 88196-70-7

science Other reagents with same CAS 88196-70-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.21 g/mol
Formula C₉H₁₃NO
badge Registry Numbers
MDL Number MFCD00671655
thermostat Physical Properties
Boiling Point 234.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a chiral building block, specifically the (R)-enantiomer, in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antidepressants. Its enantiomeric purity makes it valuable for creating active ingredients with high selectivity and reduced side effects. Commonly employed in asymmetric synthesis to introduce chirality into more complex molecules. Also utilized in the preparation of bioactive compounds and intermediates for drug discovery research.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿940.00
1g
10-20 days ฿1,940.00
5g
10-20 days ฿9,100.00
25g
10-20 days ฿43,550.00
(R)-1-(3-Methoxyphenyl)ethanamine
No image available

Used as a chiral building block, specifically the (R)-enantiomer, in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antidepressants. Its enantiomeric purity makes it valuable for creating active ingredients with high selectivity and reduced side effects. Commonly employed in asymmetric synthesis to introduce chirality into more complex molecules. Also utilized in the preparation of bioactive compounds and intermediates for drug discovery research.

Used as a chiral building block, specifically the (R)-enantiomer, in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antidepressants. Its enantiomeric purity makes it valuable for creating active ingredients with high selectivity and reduced side effects. Commonly employed in asymmetric synthesis to introduce chirality into more complex molecules. Also utilized in the preparation of bioactive compounds and intermediates for drug discovery research.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...